Induction of pro-inflammatory genes by serum amyloid A1 in human amnion fibroblasts

Abstract Serum amyloid A1 (SAA1) is an acute response protein, which is mainly produced by the liver, during infection. However, it remains unknown whether SAA1 can be produced in human fetal membranes where it is able to elicit events pertinent to labor initiation. We demonstrated that SAA1 was exp...

Full description

Bibliographic Details
Main Authors: Wenjiao Li, Wangsheng Wang, Rujuan Zuo, Chao Liu, Qun Shu, Hao Ying, Kang Sun
Format: Article
Language:English
Published: Nature Publishing Group 2017-04-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-017-00782-9
id doaj-6221e152047c4d1dbea791c86caec8d4
record_format Article
spelling doaj-6221e152047c4d1dbea791c86caec8d42020-12-08T01:32:38ZengNature Publishing GroupScientific Reports2045-23222017-04-017111210.1038/s41598-017-00782-9Induction of pro-inflammatory genes by serum amyloid A1 in human amnion fibroblastsWenjiao Li0Wangsheng Wang1Rujuan Zuo2Chao Liu3Qun Shu4Hao Ying5Kang Sun6Center for Reproductive Medicine, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong UniversityCenter for Reproductive Medicine, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong UniversityCenter for Reproductive Medicine, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong UniversityCenter for Reproductive Medicine, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong UniversityDepartment of Obstetrics and Gynecology, Zhongshan Hospital, Fudan UniversityShanghai First Maternity and Infant Hospital, Tongji University School of MedicineCenter for Reproductive Medicine, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong UniversityAbstract Serum amyloid A1 (SAA1) is an acute response protein, which is mainly produced by the liver, during infection. However, it remains unknown whether SAA1 can be produced in human fetal membranes where it is able to elicit events pertinent to labor initiation. We demonstrated that SAA1 was expressed in the fibroblasts and epithelium of the amnion and the trophoblasts of the chorion. Further study in human amnion fibroblasts showed that SAA1 production was augmented by interleukin-1β (IL-1β) and cortisol alone and synergistically, and SAA1 in turn induced the expression of IL-1β, interleukin-6 (IL-6), cyclooxygenase-2 (COX-2) and PGE2 production. These effects of SAA1 were mediated through activation of the NF-κB, p38 and ERK1/2 pathways via the toll-like receptor 4 (TLR4). Inhibition of TLR4 attenuated not only SAA1-induced activation of NF-κB, p38 and ERK1/2 but also increases in IL-1β, IL-6 and COX-2 expression. Moreover, SAA1 expression was increased in human amnion tissue following spontaneous labor. In conclusion, this study has demonstrated for the first time that SAA1 can be produced in human fetal membranes, which can be greatly induced in the presence of proinflammatory cytokines and glucocorticoids thereby producing effects associated with parturition.https://doi.org/10.1038/s41598-017-00782-9
collection DOAJ
language English
format Article
sources DOAJ
author Wenjiao Li
Wangsheng Wang
Rujuan Zuo
Chao Liu
Qun Shu
Hao Ying
Kang Sun
spellingShingle Wenjiao Li
Wangsheng Wang
Rujuan Zuo
Chao Liu
Qun Shu
Hao Ying
Kang Sun
Induction of pro-inflammatory genes by serum amyloid A1 in human amnion fibroblasts
Scientific Reports
author_facet Wenjiao Li
Wangsheng Wang
Rujuan Zuo
Chao Liu
Qun Shu
Hao Ying
Kang Sun
author_sort Wenjiao Li
title Induction of pro-inflammatory genes by serum amyloid A1 in human amnion fibroblasts
title_short Induction of pro-inflammatory genes by serum amyloid A1 in human amnion fibroblasts
title_full Induction of pro-inflammatory genes by serum amyloid A1 in human amnion fibroblasts
title_fullStr Induction of pro-inflammatory genes by serum amyloid A1 in human amnion fibroblasts
title_full_unstemmed Induction of pro-inflammatory genes by serum amyloid A1 in human amnion fibroblasts
title_sort induction of pro-inflammatory genes by serum amyloid a1 in human amnion fibroblasts
publisher Nature Publishing Group
series Scientific Reports
issn 2045-2322
publishDate 2017-04-01
description Abstract Serum amyloid A1 (SAA1) is an acute response protein, which is mainly produced by the liver, during infection. However, it remains unknown whether SAA1 can be produced in human fetal membranes where it is able to elicit events pertinent to labor initiation. We demonstrated that SAA1 was expressed in the fibroblasts and epithelium of the amnion and the trophoblasts of the chorion. Further study in human amnion fibroblasts showed that SAA1 production was augmented by interleukin-1β (IL-1β) and cortisol alone and synergistically, and SAA1 in turn induced the expression of IL-1β, interleukin-6 (IL-6), cyclooxygenase-2 (COX-2) and PGE2 production. These effects of SAA1 were mediated through activation of the NF-κB, p38 and ERK1/2 pathways via the toll-like receptor 4 (TLR4). Inhibition of TLR4 attenuated not only SAA1-induced activation of NF-κB, p38 and ERK1/2 but also increases in IL-1β, IL-6 and COX-2 expression. Moreover, SAA1 expression was increased in human amnion tissue following spontaneous labor. In conclusion, this study has demonstrated for the first time that SAA1 can be produced in human fetal membranes, which can be greatly induced in the presence of proinflammatory cytokines and glucocorticoids thereby producing effects associated with parturition.
url https://doi.org/10.1038/s41598-017-00782-9
work_keys_str_mv AT wenjiaoli inductionofproinflammatorygenesbyserumamyloida1inhumanamnionfibroblasts
AT wangshengwang inductionofproinflammatorygenesbyserumamyloida1inhumanamnionfibroblasts
AT rujuanzuo inductionofproinflammatorygenesbyserumamyloida1inhumanamnionfibroblasts
AT chaoliu inductionofproinflammatorygenesbyserumamyloida1inhumanamnionfibroblasts
AT qunshu inductionofproinflammatorygenesbyserumamyloida1inhumanamnionfibroblasts
AT haoying inductionofproinflammatorygenesbyserumamyloida1inhumanamnionfibroblasts
AT kangsun inductionofproinflammatorygenesbyserumamyloida1inhumanamnionfibroblasts
_version_ 1724394779381334016